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Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic ALCOHOL 62 mL/100mL Aerosol, Foam, 222 mL — NDC 23667-104-00 (Billing 23667-0104-00)

by Formulated Solutions, LLC · 222 mL in 1 CAN

This is a package of 222 mL of Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic ALCOHOL 62 mL/100mL Aerosol, Foam from Formulated Solutions, LLC, no longer marketed (first marketed Feb 2021), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 23667-0104-00
🏷️ FDA NDC (as labeled) 23667-104-00 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 9, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Mar 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 23667-104-00
Product NDC 23667-104
11-digit billing NDC 23667010400
RxCUI 616763
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID bc7e624c-0ee4-b6b5-e053-2a95a90abf8d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Mar 2026)
Marketing start 2021-02-09
Route TOPICAL
Dosage form AEROSOL, FOAM
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 616763
Why two NDCs? The FDA registers this code as 23667-104-00 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 23667-0104-00. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

RxNorm drug class

This medicine belongs to the Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants, Antidotes, Nerve depressants
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol guide →

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer gPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
23667-0104-00 You're viewing this Main listing 222 mL in 1 CAN 2021-02-09 — Discontinued by firm

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Alcare OR Foamed Antiseptic Handrub 62 g/100g 11084-0802-80 SC 482 g — — FDA listed —
Alcare Plus Foamed Antiseptic Handrub 62 g/100g 11084-0803-36 SC 255 g — — FDA listed —
FoamFresh Alco-Foam Hand Sanitizer 62 mL/100mL 11429-1004-00 Woodbine 400 ml — — FDA listed —
Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic 62 mL/100mLthis 23667-0104-00 Formulated 222 ml — — Discontinued —
Symmetry Foaming Hand Sanitizer 62 mL/100mL 30805-0003-03 Buckeye 2000 ml — — FDA listed —
Symmetry Foaming Hand Sanitizer-Fragrance Free with Aloe and Vitamin E 62 mL/100mL 30805-0009-04 Buckeye 1200 ml — — FDA listed —
Altra Foaming Hand Sanitizer with Aloe and Vitamin E 62 mL/100mL 30805-0012-04 Buckeye 1200 ml — — FDA listed —
Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 62 mL/100mL 30805-0013-04 Buckeye 1200 ml — — FDA listed —
Hand Guard Foaming Alcohol Instant Hand Sanitizer 620 mL/L 31507-0024-24 Wechem, 1 l — — FDA listed —
Hand Guard Foaming Instant Hand Sanitizer .62 mL/mL 31507-0585-08 Wechem, 1000 ml — — FDA listed —
Ecolab 62 mL/100mL 47593-0472-41 Ecolab 750 ml — — FDA listed —
eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL 50865-0688-09 Kutol 3785 ml — — FDA listed —
Amcon Labs Hand Sanitizer Instant Foam Sanitizer with Alcohol 620 mL/L 51801-0366-18 Nomax, 55 l — — FDA listed —
Scott Moisturizing Foam Hand Sanitizer 62 mL/100mL 55118-0546-63 Kimberly-Clark 6 bottles — — FDA listed —
Foaming Mousse Anti-Bacterial Hand Sanitizer Cherry Scented 62 mL/100mL 56136-0021-01 Ganzhou 50 ml — — FDA listed —
Foaming Mousse Anti-Bacterial Hand Sanitizer Pineapple Scented 62 mL/100mL 56136-0022-01 Ganzhou 50 ml — — FDA listed —
Foaming Mousse Anti-Bacterial Hand Sanitizer Pink Grapefruit Scented 62 mL/100mL 56136-0023-01 Ganzhou 50 ml — — FDA listed —
Alpet E3 Hand Sanitizer Foam 62 mL/100mL 59900-0125-02 Best 208197 ml — — FDA listed —
Simple Hygiene foaming hand Sanitizer 62 .62 mL/mL 60933-0062-01 FULLER 1000 ml — — FDA listed —
Simple Hygiene Hand Sanitizer 620 mg/mL 60933-0220-00 FULLER 1000 ml — — FDA listed —
Foaming Alcohol Hand Sanitizer .62 mL/mL 63900-0002-00 Simoniz 1000 ml — — FDA listed —
Soft Care Foam Instant Hand Sanitizer 62 mL/100mL 64536-7295-04 Diversey, 532 ml — — FDA listed —
WhiskCare 373 620 mL/L 65585-0374-01 Whisk 1 l — — Discontinued —
Aire-Master Foaming Hand Sanitizer Fragrance Free 620 mL/L 65585-0524-01 Whisk 3.785 l — — FDA listed —
Avant Foaming Hand Sanitizer 62 mL/100mL 68306-0109-01 B4 530 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 69674-0100-01 Saraya 500 ml — — FDA listed —
Servo Stat-Foam 62 mL/100mL 76378-0011-01 Enzyme 59 ml — — FDA listed —
Hillyard Foaming Instant Hand Sanitizer 62 mL/100mL 76402-0410-02 Hillyard 1000 ml — — FDA listed —
CleanGenic Foaming Hand Sanitizer 62 mL/100mL 81385-0000-01 CleanGenic, 3790 ml — — FDA listed —
CleanGenic 1 GALLON HAND SANITIZER 62 mL/100mL 81385-0001-04 CleanGenic, 24 bottles — — FDA listed —
CleanGenic Foaming Hand Sanitizer 62 mL/100mL 81385-0002-08 CleanGenic, 237 ml — — FDA listed —
CleanGenic 8 OZ HAND SANITIZER 62 mL/100mL 81385-0003-08 CleanGenic, 24 bottles — — FDA listed —
Transcend Alco-Foam Hand Sanitizer 62 mL/100mL 81792-0001-01 Von 1250 ml — — FDA listed —
Harbor Mist Alco-Foam Hand Sanitizer 62 mL/100mL 81792-0003-01 Von 1250 ml — — FDA listed —
Septihol Hand Sanitizer 62 mL/100mL 00519-6257-35 STERIS 24 bottles — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2021
On the market since
Feb 2021
📍
2026
Currently FDA-listed
5 years listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

Manufacturer & labeler

LabelerFormulated Solutions, LLC
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code23667
First marketedFeb 2021
Product typeHuman Otc Drug
Portfolio26 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 21 words ▾

Uses(s) Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

⏱️ Dosage and Administration 37 words ▾

Directions Hold can upside down and dispense into palm. Place enough product on hands to cover all surfaces. Rub hands together until dry Supervise children under 6 years of age when using this product to avoid swallowing.

⚠️ Warnings 112 words ▾

Warnings For external use only. Extermely flammable, do not use near heat or flame or while smoking. Do not use On children less than 2 months of age On open skin wounds When using this product keep out of eyes, ears, and mouth In case of contact with eyes, rinse eyes thoroughly with water.

Do not puncture or incinerate Contents under pressure Do not expose to heat or store at temperature above 120°F (49°C) Stop use and ask a doctor If irritation or rash occurs. These may be signs of a serious condition. Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 8 words ▾

Active ingredient Ethyl Alcohol 62% v/v Purpose Antiseptic

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients Purified Water, Hydrofluorocarbon 152a; Isobutane; Emulsifying Wax NF; Propane

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Do Not Use 15 words ▾

Do not use On children less than 2 months of age On open skin wounds

📄 When Using This Product 42 words ▾

When using this product keep out of eyes, ears, and mouth In case of contact with eyes, rinse eyes thoroughly with water. Do not puncture or incinerate Contents under pressure Do not expose to heat or store at temperature above 120°F (49°C)

📄 Stop Use and Ask a Doctor If 19 words ▾

Stop use and ask a doctor If irritation or rash occurs. These may be signs of a serious condition.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 3 words ▾

Package Labeling: Bottle2

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
Who lists this product with the FDA?
Formulated Solutions, LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.
← 23667-0103-00 · Formulated 23667-0800-01 · Formulated →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.